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Polymorphic regulation of mitochondrial fission and fusion modifies phenotypes of microglia in neuroinflammation

Microglia are the resident macrophages of the central nervous system and play complex roles in the milieu of diseases including the primary diseases of myelin. Although mitochondria are critical for cellular functions and survival in the nervous system, alterations in and the roles of mitochondrial...

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Autores principales: Katoh, Mitsuhiko, Wu, Bao, Nguyen, Huy Bang, Thai, Truc Quynh, Yamasaki, Ryo, Lu, Haiyan, Rietsch, Anna M., Zorlu, Musab M., Shinozaki, Youichi, Saitoh, Yurika, Saitoh, Sei, Sakoh, Takashi, Ikenaka, Kazuhiro, Koizumi, Schuichi, Ransohoff, Richard M., Ohno, Nobuhiko
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5503944/
https://www.ncbi.nlm.nih.gov/pubmed/28694451
http://dx.doi.org/10.1038/s41598-017-05232-0
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author Katoh, Mitsuhiko
Wu, Bao
Nguyen, Huy Bang
Thai, Truc Quynh
Yamasaki, Ryo
Lu, Haiyan
Rietsch, Anna M.
Zorlu, Musab M.
Shinozaki, Youichi
Saitoh, Yurika
Saitoh, Sei
Sakoh, Takashi
Ikenaka, Kazuhiro
Koizumi, Schuichi
Ransohoff, Richard M.
Ohno, Nobuhiko
author_facet Katoh, Mitsuhiko
Wu, Bao
Nguyen, Huy Bang
Thai, Truc Quynh
Yamasaki, Ryo
Lu, Haiyan
Rietsch, Anna M.
Zorlu, Musab M.
Shinozaki, Youichi
Saitoh, Yurika
Saitoh, Sei
Sakoh, Takashi
Ikenaka, Kazuhiro
Koizumi, Schuichi
Ransohoff, Richard M.
Ohno, Nobuhiko
author_sort Katoh, Mitsuhiko
collection PubMed
description Microglia are the resident macrophages of the central nervous system and play complex roles in the milieu of diseases including the primary diseases of myelin. Although mitochondria are critical for cellular functions and survival in the nervous system, alterations in and the roles of mitochondrial dynamics and associated signaling in microglia are still poorly understood. In the present study, by combining immunohistochemistry and 3D ultrastructural analyses, we show that mitochondrial fission/fusion in reactive microglia is differentially regulated from that in monocyte-derived macrophages and the ramified microglia of normal white matter in myelin disease models. Mouse cerebral microglia in vitro demonstrated that stimulation of TLR4 with lipopolysaccharide, widely used to examine microglial reactions, caused the activation of the mitochondrial fission protein, dynamin-related protein 1 (Drp1) and enhanced production of reactive oxygen species (ROS). The increase in the ROS level activated 5′ adenosine monophosphate-activated protein kinase (AMPK), and facilitated elongation of mitochondria along the microtubule tracks. These results suggest that the polymorphic regulation of mitochondrial fission and fusion in reactive microglia is mediated by distinct signaling under inflammatory conditions, and modulates microglial phenotypes through the production of ROS.
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spelling pubmed-55039442017-07-12 Polymorphic regulation of mitochondrial fission and fusion modifies phenotypes of microglia in neuroinflammation Katoh, Mitsuhiko Wu, Bao Nguyen, Huy Bang Thai, Truc Quynh Yamasaki, Ryo Lu, Haiyan Rietsch, Anna M. Zorlu, Musab M. Shinozaki, Youichi Saitoh, Yurika Saitoh, Sei Sakoh, Takashi Ikenaka, Kazuhiro Koizumi, Schuichi Ransohoff, Richard M. Ohno, Nobuhiko Sci Rep Article Microglia are the resident macrophages of the central nervous system and play complex roles in the milieu of diseases including the primary diseases of myelin. Although mitochondria are critical for cellular functions and survival in the nervous system, alterations in and the roles of mitochondrial dynamics and associated signaling in microglia are still poorly understood. In the present study, by combining immunohistochemistry and 3D ultrastructural analyses, we show that mitochondrial fission/fusion in reactive microglia is differentially regulated from that in monocyte-derived macrophages and the ramified microglia of normal white matter in myelin disease models. Mouse cerebral microglia in vitro demonstrated that stimulation of TLR4 with lipopolysaccharide, widely used to examine microglial reactions, caused the activation of the mitochondrial fission protein, dynamin-related protein 1 (Drp1) and enhanced production of reactive oxygen species (ROS). The increase in the ROS level activated 5′ adenosine monophosphate-activated protein kinase (AMPK), and facilitated elongation of mitochondria along the microtubule tracks. These results suggest that the polymorphic regulation of mitochondrial fission and fusion in reactive microglia is mediated by distinct signaling under inflammatory conditions, and modulates microglial phenotypes through the production of ROS. Nature Publishing Group UK 2017-07-10 /pmc/articles/PMC5503944/ /pubmed/28694451 http://dx.doi.org/10.1038/s41598-017-05232-0 Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Katoh, Mitsuhiko
Wu, Bao
Nguyen, Huy Bang
Thai, Truc Quynh
Yamasaki, Ryo
Lu, Haiyan
Rietsch, Anna M.
Zorlu, Musab M.
Shinozaki, Youichi
Saitoh, Yurika
Saitoh, Sei
Sakoh, Takashi
Ikenaka, Kazuhiro
Koizumi, Schuichi
Ransohoff, Richard M.
Ohno, Nobuhiko
Polymorphic regulation of mitochondrial fission and fusion modifies phenotypes of microglia in neuroinflammation
title Polymorphic regulation of mitochondrial fission and fusion modifies phenotypes of microglia in neuroinflammation
title_full Polymorphic regulation of mitochondrial fission and fusion modifies phenotypes of microglia in neuroinflammation
title_fullStr Polymorphic regulation of mitochondrial fission and fusion modifies phenotypes of microglia in neuroinflammation
title_full_unstemmed Polymorphic regulation of mitochondrial fission and fusion modifies phenotypes of microglia in neuroinflammation
title_short Polymorphic regulation of mitochondrial fission and fusion modifies phenotypes of microglia in neuroinflammation
title_sort polymorphic regulation of mitochondrial fission and fusion modifies phenotypes of microglia in neuroinflammation
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5503944/
https://www.ncbi.nlm.nih.gov/pubmed/28694451
http://dx.doi.org/10.1038/s41598-017-05232-0
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